LUCIA
K-Number: K102375 · 2011-02-25
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Device Summary
Frequently Asked Questions
What is the LUCIA?
LUCIA is a medical device that received FDA 510(k) clearance on 2011-02-25. The listed applicant is Meridian Co., Ltd.. The 510(k) number is K102375.
When did LUCIA receive FDA 510(k) clearance?
LUCIA received FDA 510(k) clearance on 2011-02-25, under 510(k) number K102375.
Who is the listed applicant for LUCIA?
The FDA 510(k) record lists Meridian Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUCIA?
The FDA product code for LUCIA is ILY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Meridian Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ILY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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